Ink jet ink, ink set, ink jet recording method, ink cartridge, recording unit, and ink jet recording apparatus

ABSTRACT

An ink jet ink is disclosed which includes water, a water-soluble organic solvent and a coloring material and has excellent properties. The coloring material is a specific phthalocyanine derivative and is contained in a specific amount in the ink. The water-soluble organic solvent includes a specific amount of 2-pyrrolidone. In addition, a d 75  value is in a specific range where the d 75  value corresponds to 75% of a dispersion distance distribution, measured by a small angle X-ray scattering method, of molecular aggregates in the ink jet ink whose coloring material concentration is adjusted to 0.5 mass %.

This application is a continuation of International Application No.PCT/JP2005/012709 filed on Jul. 4, 2005, which claims the benefit ofJapanese Patent Application No. 2004-196451 filed on Jul. 2, 2004, andNo. 2005-192190 filed on Jun. 30, 2005.

BACKGROUND OF THE INVENTION

1. Field of the Invention

The present invention relates to an ink jet ink which has highenvironmental gas resistance and provides good images in which theoccurrence of metallic luster, the so-called bronze phenomenon, issuppressed even when the ink is printed on a recording medium. Thepresent invention also relates to an ink set, an ink jet recordingmethod, an ink cartridge, a recording unit, and an ink jet recordingapparatus each using the ink jet ink.

2. Related Background Art

An ink jet recording method is a recording method of applying a smallink droplet to any one of recording media such as plain paper and glossymedia to form an image, and has become rapidly widespread owing toreduction in costs and improvement in recording rate. With the rapidspread of digital cameras in addition to improvement in the quality ofimages recorded by the method, the method has been generally used as amethod of outputting photographic images comparable to silver halidephotograph.

In recent years, image quality has undergone improvement more than everowing to, for example, extreme reduction in size of an ink droplet andan improvement of the color gamut involved in the introduction ofmulti-color ink. Meanwhile, there have been growing demands for coloringmaterials and inks, and stricter properties have been required inrespect of improvement of color developability and reliabilityconcerning anti-clogging or ejection stability.

As compared with the silver halide photograph, the ink jet recordingmethod is problematic in respect of, for example, the image storagestability of the resultant recorded product. In general, the recordedproduct obtained by the ink jet recording method is inferior in imagestorage stability to that by the silver halide photograph, and involvesthe emergence of a problem in that a coloring material on the recordedproduct is apt to deteriorate to cause a change in the color tone of theimage and the color fading of the image when the recorded product isexposed to light, heat, environmental gases present in the air, or thelike for a long period of time. In particular, the enhancement ofenvironmental gas resistance to the level of silver halide photographhas been of a concern from the past in the ink jet recording method.Cyan has the lowest environmental gas resistance among yellow, magenta,and cyan, which are hues used for ink jet ink. Therefore, theenhancement of the environmental gas resistance of cyan ink to the levelcomparable to that of yellow ink or magenta ink is of one importantconcern in the ink jet recording method.

The basic skeletons of coloring materials for ink jet ink having a cyanhue are roughly classified into a phthalocyanine skeleton and atriphenylmethane skeleton. Representative coloring materials of theformer include C.I. Direct Blue 86 and 87, and C.I. Direct Blue 199.Representative coloring materials of the latter include C.I. Acid Blue9.

In general, a phthalocyanine-based coloring material is characterized inthat it is excellent in light resistance as compared with atriphenylmethane-based coloring material. Furthermore, thephthalocyanine-based coloring material has high fastness propertiesagainst humidity or heat and has good color developability, and so thecoloring material has been widely used as a coloring material for inkjet ink.

However, the phthalocyanine-based coloring material tends to be poor infastness against environmental gases in the air (such as ozone, No_(x),or SO₂), especially an ozone gas. In particular, in a recorded productobtained by applying the coloring material on a recording medium havingan ink-receiving layer containing an inorganic substance such as aluminaor silica, the fastness is significantly low, hence the color fading ofthe recorded product is remarkable when the recorded product is leftstanding in a room for a long period of time. Various compounds to beadded to ink have been disclosed for the purpose of improving theenvironmental gas resistance (see, for example, Japanese PatentApplication Laid-Open No. H05-171085, Japanese Patent ApplicationLaid-Open No. H11-29729, Japanese Patent Application Laid-Open No.H10-130517, Japanese Patent Application Laid-Open No. 2000-303009, andJapanese Patent Application Laid-Open No. 2002-249677). However, none ofthose publications has achieved compatibility between good colordevelopability and high environmental gas resistance for ink jet ink.

The phthalocyanine-based coloring material involves another problem,that is, the occurrence of metallic luster resulting from the highaggregation properties of the coloring material, the so-called bronzephenomenon. When the bronze phenomenon occurs in a recorded product, theoptical reflection properties of the recorded product change. As aresult, the color developability and hue of an image remarkably change,with the result that the image quality is significantly lowered. Thebronze phenomenon is considered to occur as a result of the aggregationof the coloring material on the surface of a recording medium due to,for example, the high aggregation properties of the coloring material inink and a lowering in permeability of the ink into the recording mediumwhen the ink is applied to the recording medium. In particular, acoloring material with an amino group introduced in its molecule for thepurpose of improving environmental gas resistance, or an ink containinga coloring material having low solubility in water tends tosignificantly cause the bronze phenomenon.

For example, it has been proposed that a specific phthalocyanine-basedcoloring material is used to improve the environmental gas resistance(see, for example, Japanese Patent No. 2942319). The use of the specificphthalocyanine-based coloring material provides the environmental gasresistance which is of one concern in the phthalocyanine-based coloringmaterial. However, in the proposition, there is no reference to thebronze phenomenon, and hence, resistance to the bronze phenomenon of thecoloring material is unclear. In other words, the compatibility betweenresistance to bronze phenomenon (bronze resistance) and environmentalgas resistance has not yet been achieved.

Therefore, it is indispensable to conduct research on ink jet ink usinga phthalocyanine-based coloring material which is excellent in colordevelopability, has high environmental gas resistance, and suppressesthe occurrence of the bronze phenomenon.

SUMMARY OF THE INVENTION

In view of the above problems, the inventors of the present inventionhave made extensive studies. As a result, the inventors have found thatink jet ink which is excellent in color developability, has highenvironmental gas resistance, and is capable of providing imagesexcellent in bronze resistance can be provided by using a specificphthalocyanine-based coloring material and controlling the aggregationproperties of the coloring material, thereby completing the presentinvention.

Therefore, an object of the present invention is to provide an ink jetink which is excellent in color developability, has high environmentalgas resistance, and is capable of providing images excellent in bronzeresistance.

Other objects of the present invention are to provide a recordingmethod, a recording unit, an ink cartridge, and an ink jet recordingapparatus each using the ink jet ink.

The above objects are achieved by the present invention described below.That is, according to one aspect of the present invention, an ink jetink is provided comprising at least water, a water-soluble organicsolvent and a coloring material, wherein the coloring material is acompound represented by the following general formula (I) or a saltthereof; a content (mass %) of the coloring material is 0.5 mass % ormore and less than 3.0 mass % with respect to a total mass of the inkjet ink; and a content (mass %) of 2-pyrrolidone in the water-solubleorganic solvent is 50.0% or more with respect to the content (mass %) ofthe coloring material; and in a dispersion distance distribution,measured by a small-angle X-ray scattering method, of molecularaggregates in the ink jet ink whose coloring material concentration isadjusted to 0.5 mass %, a dispersion distance d₇₅ value corresponding to75% of the distribution is 6.70 nm or more and 10.60 nm or less:

(wherein M represents an alkali metal or ammonium; R₁ and R₂ eachindependently represent a hydrogen atom, a sulfonic group, or a carboxylgroup (provided that R₁ and R₂ are not simultaneously a hydrogen atom);Y represents a chlorine atom, a hydroxyl group, an amino group, or amonoalkylamino or dialkylamino group; 1 represents 0 to 2, m represents1 to 3, and n represents 1 to 3 (provided that 1+m+n=3 to 4); andpositions at which the substituents are present are the 4- or41-positions).

According to another aspect of the present invention, an ink jet ink isprovided containing at least water, a water-soluble organic solvent anda coloring material, wherein the coloring material is a compoundrepresented by the following general formula (I) or a salt thereof; acontent (mass %) of the coloring material is 0.5 mass % or more and lessthan 3.0 mass % with respect to a total mass of the ink jet ink; and acontent (mass %) of 2-pyrrolidone in the water-soluble organic solventis 50.0% or more with respect to a content (mass %) of the coloringmaterial; and a maximum absorption wavelength (λmax) obtained bymeasuring an absorbance of an ink prepared by diluting 2,000 times theink jet ink is 608.0 nm or more and 613.0 nm or less:

(wherein M represents an alkali metal or ammonium; R₁ and R₂ eachindependently represent a hydrogen atom, a sulfonic group, or a carboxylgroup (provided that R₁ and R₂ are not simultaneously a hydrogen atom);Y represents a chlorine atom, a hydroxyl group, an amino group, or amonoalkylamino or dialkylamino group; 1 represents 0 to 2, m represents1 to 3, and n represents 1 to 3 (provided that 1+m+n=3 to 4); andpositions at which the substituents are present are the 4- or4′-positions.)

In another aspect of the ink jet ink, the coloring material is acompound represented by the following general formula (II) or a saltthereof:

(wherein M represents an alkali metal or ammonium; 1 represents 0 to 2,m represents 1 to 3, and n represents 1 to 3 (provided that 1+m+n=3 to4); and positions at which the substituents are present are the 4- or4′-positions).

According to another aspect of the present invention, an ink jetrecording method is provided including ejecting an ink by an ink jetmethod to perform recording on a recording medium, wherein the ink isthe above-described ink jet ink.

According to another aspect of the present invention, an ink cartridgeis provided including an ink storage portion for storing an ink, whereinthe ink is the above-described ink jet ink.

According to another aspect of the present invention, a recording unitis provided including an ink storage portion for storing an ink and arecording head for ejecting the ink, wherein the ink is theabove-described ink jet ink.

According to another aspect of the present invention, an ink jetrecording apparatus is provided including an ink storage portion forstoring an ink and a recording head for ejecting the ink, wherein theink is the above-described ink jet ink.

According to the present invention, an ink jet ink can be provided whichis excellent in color developability, has high environmental gasresistance, and is capable of providing an image excellent in bronzeresistance.

According to the present invention, an ink jet recording method, an inkcartridge, a recording unit, and an ink jet recording apparatus eachusing the ink jet ink can be provided.

BRIEF DESCRIPTION OF THE DRAWINGS

FIG. 1 is a view showing the measurement principle of a small-angleX-ray scattering method;

FIG. 2 is a small-angle X-ray scattering profile of each of aphthalocyanine-based coloring material and a triphenylmethane-basedcoloring material;

FIG. 3 is a conceptual diagram of the dispersion distance betweenmolecular aggregates of a phthalocyanine-based coloring material;

FIG. 4 is a perspective view of a recording apparatus;

FIG. 5 is a perspective view of a mechanism portion of the recordingapparatus;

FIG. 6 is a sectional view of the recording apparatus;

FIG. 7 is a perspective view showing a state in which an ink tank ismounted on a head cartridge;

FIG. 8 is an exploded perspective view of the head cartridge; and

FIG. 9 is a front view showing a recording element substrate in the headcartridge.

DESCRIPTION OF THE PREFERRED EMBODIMENTS

Hereinafter, the present invention will be described in more detail byway of preferred embodiments.

In the present invention, when a coloring material is a salt, the saltis dissociated into ions in ink, but this state is represented by usingthe phrase “contains a salt” for convenience.

<Ink>

Hereinafter, components constituting the ink jet ink according to thepresent invention (hereinafter also referred to simply as the ink) andthe like will be described in detail.

Among yellow ink, magenta ink and cyan ink each of which is widely usedas ink jet ink, particularly the cyan ink tends to be poor inenvironmental gas resistance. To cope with the problem of theenvironmental gas resistance in cyan ink, the present invention aims atproviding cyan ink in which, when a recorded product obtained by meansof the cyan ink is exposed to an environment having a temperature of 40°C., a humidity of 55% and an ozone gas concentration of 2 ppm for 20hours, the reflection density at a 50% duty portion of the recordedproduct is 83% or more of the reflection density at the 50% duty portionof the recorded product before the exposure. A recorded product obtainedby using yellow ink and magenta ink each excellent in environmental gasresistance has excellent environmental gas resistance with which 83% ormore of the reflection density remains under the above exposureconditions. Therefore, using cyan ink in which 83% or more of thereflection density remains under the above exposure conditions incombination with yellow ink and magenta ink each excellent inenvironmental gas resistance, excellent image storage stability can beachieved.

(Coloring Material)

[Compound Represented by General Formula (I) or a Salt Thereof]

The ink according to the present invention must contain a compoundrepresented by the following general formula (I) or a salt thereof. Thecompound represented by the following general formula (I) or the saltthereof is a phthalocyanine derivative characterized in that it has acyan hue and is excellent in environmental gas resistance.

(In the general formula (I), M represents an alkali metal or ammonium;R₁ and R₂ each independently represent a hydrogen atom, a sulfonicgroup, or a carboxyl group (provided that R₁ and R₂ are notsimultaneously a hydrogen atom); Y represents a chlorine atom, ahydroxyl group, an amino group, or a monoalkylamino or dialkylaminogroup; 1 represents 0 to 2, m represents 1 to 3, and n represents 1 to 3(provided that 1+m+n=3 to 4); and positions at which the substituentsare present are the 4- or 4′-positions.)

In general, when a phthalocyanine derivative is synthesized, it ofteninevitably includes substitution position isomers which are different inpositions at which substituents R_(n) (n: 1 to 16) in the generalformula (III) (positions of carbon atoms on the benzene rings to whichR₁ to R₁₆ are bonded are defined as 1 position to 16 position,respectively) are present. However, in general, the substitutionposition isomers are not distinguished from one another, and are oftenregarded as the same derivative.

The coloring material used in the present invention is a phthalocyaninederivative obtained by selectively introducing an unsubstitutedsulfamoyl group (—SO₂NH₂) or a substituted sulfamoyl group (a grouprepresented by the general formula (IV)) to only at each of the4-positions and 4′-positions in the general formula (I) (R₂, R₃, R₆, R₇,R₁₀, R₁₁, R₁₄, and R₁₅ in the general formula (III)). The inventors ofthe present invention have found that a recorded product obtained bymeans of an ink containing such a compound is extremely excellent inenvironmental gas resistance.

The compound represented by the general formula (I) or the salt thereofused in the present invention is synthesized by using, as a rawmaterial, a phthalocyanine compound obtained by reacting a4-sulfophthalic acid derivative, or a 4-sulfophthalic acid derivativeand a phthalic (anhydride) derivative, in the presence of a metalcompound. The compound or the salt thereof is obtained by converting asulfonic group in the phthalocyanine compound into a chlorosulfonicgroup which is then allowed to react with an aminating agent in thepresence of an organic amine.

Preferable examples of the substituted sulfamoyl group represented bythe general formula (IV) are shown below. The substituted sulfamoylgroup used in the present invention is not limited to them. Thesubstituted sulfamoyl group represented by the general formula (IV) isshown in the form of a free acid.

Of those, a compound substituted by Exemplified Substituent 1 above,that is, a compound represented by the following general formula (II) ora salt thereof is most preferable from the viewpoint of the balancebetween color developability and environmental gas resistance.

(In the general formula (II), M represents an alkali metal or ammonium;1 represents 0 to 2, m represents 1 to 3, and n represents 1 to 3(provided that 1+m+n=3 to 4); and positions at which the substituentsare present are the 4- or 4′-positions.)

However, even in such a compound as represented by the general formula(I) used in the present invention in which the number of substituents is3 to 4, that is, 1+m+n 3 to 4 and the substitution positions are limitedto the 4- or 4′-positions, a large number of isomers are present asshown in Tables 1 and 2 below, which are different from each other inthe number of each of a sulfonic group (—SO₃M), an unsubstitutedsulfamoyl group (—SO₂NH₂), and a substituted sulfamoyl group (a grouprepresented by the general formula (IV)), each of which is a substituentwith which the phthalocyanine skeleton is substituted. The compoundrepresented by the general formula (I) or the salt thereof is a mixtureof those isomers, and it has been confirmed that even compounds havingthe same structure are greatly different in their properties dependingon the number and kinds of isomers. A difference in aggregationproperties between coloring materials may be cited as one example of theproperties.

TABLE 1 The number of substituents, the positions of substituents, andthe kinds of isomers (where l + m + n = 4) Unsubstituted SubstitutedSulfonic group sulfamoyl group sulfamoyl group 4 4′ 4 4′ 4 4′ positionposition position position position position L, m, n = 0 0 1 0 3 0 0, 1,3 0 0 1 0 2 1 0 0 1 0 1 2 0 0 1 0 0 3 0 0 0 1 3 0 0 0 0 1 2 1 0 0 0 1 12 0 0 0 1 0 3 l, m, n = 0 0 2 0 2 0 0, 2, 2 0 0 2 0 1 1 0 0 2 0 0 2 0 01 1 2 0 0 0 1 1 1 1 0 0 1 1 0 2 0 0 0 2 2 0 0 0 0 2 1 1 0 0 0 2 0 2 l,m, n = 0 0 3 0 1 0 0, 3, 1 0 0 3 0 0 1 0 0 2 1 1 0 0 0 2 1 0 1 0 0 1 2 01 0 0 1 2 1 0 0 0 0 3 0 1 0 0 0 3 1 0 l, m, n = 1 0 1 0 2 0 1, 1, 2 1 01 0 1 1 1 0 1 0 0 2 1 0 0 1 2 0 1 0 0 1 1 1 1 0 0 1 0 2 0 1 1 0 2 0 0 11 0 1 1 0 1 1 0 0 2 0 1 0 1 2 0 0 1 0 1 1 1 0 1 0 1 0 2 L, m, n = 1 0 20 1 0 1, 2, 1 1 0 2 0 0 1 1 0 1 1 1 0 1 0 1 1 0 1 1 0 0 2 1 0 1 0 0 2 01 0 1 2 0 1 0 0 1 2 0 0 1 0 1 1 1 1 0 0 1 1 1 0 1 0 1 0 2 1 0 0 1 0 2 01 L, m, n = 2 0 1 0 1 0 2, 1, 1 2 0 1 0 0 1 2 0 0 1 1 0 2 0 0 1 0 1 1 11 0 1 0 1 1 1 0 0 1 1 1 0 1 1 0 1 1 0 1 0 1 0 2 1 0 1 0 0 2 1 0 0 1 0 20 1 1 0 0 2 0 1 0 1

TABLE 2 The number of substituents, the positions of substituents, andthe kinds of isomers (where l + m + n = 3) Unsubstituted SubstitutedSulfonic group sulfamoyl group sulfamoyl group 4 4′ 4 4′ 4 4′ positionposition position position position position L, m, n = 0 0 1 0 2 0 0, 1,2 0 0 1 0 1 1 0 0 1 0 0 2 0 0 0 1 2 0 0 0 0 1 1 1 0 0 0 1 0 2 l, m, n =0 0 2 0 1 0 0, 2, 1 0 0 2 0 0 1 0 0 1 1 1 0 0 0 1 1 0 1 0 0 0 2 1 0 0 00 2 0 1 l, m, n = 1 0 1 0 1 0 1, 1, 1 1 0 1 0 0 1 1 0 0 1 1 0 1 0 0 1 01 0 1 1 0 1 0 0 1 1 0 0 1 0 1 0 1 1 0 0 1 0 1 0 1

In general, a phthalocyanine-based coloring material has higheraggregation properties than coloring materials having other structures(for example, a triphenylmethane-based, azo-based, or xanthene-basedcoloring material). The enhancement of the aggregation propertieselevates fastness. Meanwhile, coloring materials having high aggregationproperties shows high aggregation properties also in ink. Therefore,when an image is printed on a recording medium by using such coloringmaterials, the bronze phenomenon tends to remarkably occur to lowerimage quality.

In contrast, when a coloring material has significantly low aggregationproperties, the fastness properties (especially environmental gasresistance) of the coloring material deteriorate. Therefore, therecorded product obtained by using an ink containing such a coloringmaterial may be unable to obtain image storage stability at the samelevel as yellow ink and magenta ink which are excellent in environmentalgas resistance.

Accordingly, when the compound represented by the general formula (I) orthe salt thereof is used as a coloring material, the aggregationproperties of the coloring material must be controlled in such a mannerthat the occurrence of the bronze phenomenon can be suppressed anddesired environmental gas resistance can be obtained.

In recent years, in order to obtain high-quality images comparable tosilver halide photograph, image formation has often been performed byusing multiple inks having the same color tone and different coloringmaterial concentrations in combination. In other words, an ink having arelatively high coloring material content (a so-called deep-color ink)and an ink having a relatively low coloring material content (aso-called light-color ink) are used in combination. When using adeep-color ink and a light-color ink in combination, an image withreduced granularity of a light-color portion and excellent gradation canbe formed. However, the investigation by the inventors of the presentinvention has revealed that images formed by using light-color ink maybe inferior in environmental gas resistance to images formed by means ofdeep-color ink.

In particular, in ink containing a phthalocyanine-based coloringmaterial, the problem concerning poor fastness is expected to be solvedby increasing the aggregation properties of the coloring material.However, it has been found that the bronze phenomenon occurs even inlight-color ink having a relatively low coloring material concentration,specifically light-color ink having a coloring material content of 0.5mass % or more and less than 3.0 mass % with respect to the total massof the ink when the aggregation properties of a coloring material isincreased.

On the basis of the above finding, the inventors of the presentinvention have concentrated their attention on the aggregationproperties of the compound represented by the general formula (I) or thesalt thereof, and made extensive studies. As a result, the inventorshave found a method in which: kinds of substituents of the compoundrepresented by the general formula (I) or the salt thereof as a coloringmaterial in ink having a coloring material content (mass %) of 0.5 mass% or more and less than 3.0 mass % with respect to the total mass of theink are changed to control the aggregation properties of the coloringmaterial; and 2-pyrrolidone, which is a water-soluble organic solventparticularly effective in suppressing the occurrence of the bronzephenomenon in the compound represented by the general formula (I) or thesalt thereof, is used in combination with the compound to provideexcellent color developability, suppress the occurrence of the bronzephenomenon, and enhance environmental gas resistance. Thus, theinventors have completed the present invention.

[Measurement of Aggregation Properties of Coloring Material]

A small-angle X-ray scattering method is applicable to the measurementof the aggregation properties of a coloring material used in the presentinvention.

As described in, for example, “Saishin Colloid Kagaku” (Latest ColloidChemistry) (Kodansha Scientific, Fumio Kitahara and Kunio Furusawa) and“Hyomen Jotai and Colloid Jotai” (Surface State and Colloid State)(Tokyo Kagaku Dozin, Co., Ltd., Masayuki Nakagaki), the small-angleX-ray scattering method is an approach that has been generally used forcalculating a distance between colloid particles in a colloidalsolution.

The outline of a small-angle X-ray scattering apparatus will bedescribed with reference to FIG. 1 showing the measurement principle ofthe small-angle X-ray scattering method. The focal spot size of each ofX-rays generated from an X-ray source is reduced to about severalmillimeters during the passing of the X-rays through first to thirdslits, and a sample solution is irradiated with the X-rays. The X-rayswith which the sample solution is irradiated are scattered by particlesin the sample solution before the X-rays are detected on an imagingplate. Since the scattered X-rays interfere with each other because ofan optical path difference between them, a distance d value betweenparticles can be determined on the basis of a Bragg equation (thefollowing expression (1)) using the resultant θ value. When particlesare arranged to be equidistance, the d value determined here isconsidered to be a distance from the center of a particle to the centerof an adjacent particle.d=λ/2 sin θ  Eq. (1)(In the expression (1), λ represents the wavelength of an X-ray, drepresents the distance between particles, and θ represents a scatteringangle.)

In general, no peak occurs in a scattering angle profile when particlesin a solution are not regularly arranged. In the case of an aqueoussolution of the coloring material (phthalocyanine-based coloringmaterial) used in the present invention, a strong peak having themaximum value in the range of 2θ=0° to 5° is detected, and particles(molecular aggregates) formed by aggregation of phthalocyanine-basedcoloring material molecules are found to be arranged by a certainregulation. FIG. 2 shows the scattering angle profile in a 10-mass %aqueous solution of each of a triphenylmethane-based coloring materialhaving a structure represented by Compound (1) below and aphthalocyanine-based coloring material having the structure representedby the general formula (I). FIG. 2 shows that phthalocyanine-basedcoloring materials specifically have scattering angle peaks even whenthey have the same cyan hue. In other words, several phthalocyaninemolecules are aggregated in an aqueous solution of aphthalocyanine-based coloring material to form molecular aggregates. Inaddition, the distances between the molecular aggregates have such aconstant distribution as represented by a scattering angle profile.

FIG. 3 is a schematic view of the dispersion distance between molecularaggregates of a phthalocyanine-based coloring material. As shown in FIG.3, the radius of a certain molecular aggregate of thephthalocyanine-based coloring material is denoted by r1 and the distancebetween molecular aggregates is denoted by d1. Assuming that d1 isalways constant when the structure of the phthalocyanine-based coloringmaterial remains unchanged, the d value measured by a small-angle X-rayscattering method is considered to increase from d2 to d3 as the radiusof the molecular aggregate formed by the phthalocyanine-based coloringmaterial increases from r1 to r2. Accordingly, the d value measured bythe above method is considered to be an indication of the size of themolecular aggregate of the phthalocyanine-based coloring material, andthe size of the molecular aggregate formed from coloring materialmolecules is considered to increase as the d value increases.

Investigation into the relationship between the d value in inkcontaining a phthalocyanine-based coloring material and the bronzephenomenon has revealed that in the case of phthalocyanine-basedcoloring materials represented by the same structural formula, thebronze phenomenon is more likely to occur as the d value is larger.Taking into consideration the fact that the bronze phenomenon occursowing to the aggregation of coloring material molecules on a recordingmedium, it has been supported that there is the correlation between thed value described above and the size of a molecular aggregate.

A peak shape in a scattering angle profile indicates the distribution ofthe distances between molecular aggregates, that is, the distribution ofthe dispersion distances between the molecular aggregates. Taking intoconsideration the above-described fact that the dispersion distances arean indication of the sizes of molecular aggregates, such scatteringangle profile is supposed to indicate the distribution of the sizes ofmolecular aggregates in a solution. In other words, assuming that thepeak area of a scattering angle profile shows the sizes of the entiremolecular aggregates in a solution, the bronze phenomenon tends to bemore likely to occur as the d value is larger, that is, the frequency oflarge molecular aggregates is higher. Therefore, reducing the frequencyof large molecular aggregates which are apt to cause the bronzephenomenon is expected to be capable of suppressing the occurrence ofthe bronze phenomenon. However, in the case of ink containing onlysignificantly small molecular aggregates, the environmental gasresistance of the ink is lowered, although the bronze phenomenon is lesslikely to occur. Accordingly, the sizes of molecular aggregates (theabsolute value of the d value) must be appropriately controlled forsuppressing the occurrence of the bronze phenomenon and for obtainingenvironmental gas resistance.

In general, when the sizes of coloring material molecules have a certainfrequency distribution, the threshold value of the visual sense which isthe limit of the observability of a human being is said to be 25% of theentire amount. In view of the above, the d value at the point at whichlarge molecular aggregates causative of the bronze phenomenon comes toaccount for 25% or less of the entire aggregates, i.e., the point atwhich small molecular aggregates which hardly cause the bronzephenomenon accounts for 75% or more of the entire aggregates is definedas a d₇₅ value and the d₇₅ value is so controlled as to fall within aspecific range, whereby ink which suppresses the occurrence of thebronze phenomenon and has high environmental gas resistance can beobtained.

In actuality, according to investigation into the correlation betweeneach of a d_(peak) value calculated from the peak of a 2θ value in ascattering angle profile and the above-described d₇₅ value, and theoccurrence level of the bronze phenomenon, it has been found that thed₇₅ value in which a distribution factor of the sizes of the entiremolecular aggregates is taken into account has a stronger correlationwith the bronze phenomenon than the d_(peak) value. A base line fordetermining the 2θ value is drawn in the range of 0.5° to 5°.

In view of the foregoing, the inventors of the present invention haveconducted the following experiment using compounds prepared by changingthe number, kinds, and substitution positions of substituents in thecompound represented by the general formula (I) or the salt thereof,which is a phthalocyanine-based coloring material, that is, coloringmaterials with the aggregation properties controlled. Inks containingthe coloring materials were prepared, and the scattering angle profilesof the inks were measured to calculate the d₇₅ values, Next, thecoloring materials were evaluated for the aggregation properties on thebasis of their respective d₇₅ values. As a result, it is confirmed that,when ink had the d₇₅ value of 6.70 nm or more and 10.60 nm or less, theink effectively suppressed the occurrence of the bronze phenomenon andhad high environmental gas resistance, and besides, that when ink hadthe d₇₅ value of 6.70 nm or more and 9.10 nm or less, the inkparticularly effectively suppressed the occurrence of the bronzephenomenon and had high environmental gas resistance. Namely, in thecase where the aggregation properties of the compound represented by thegeneral formula (I) or the salt thereof as a coloring material iscontrolled in such a manner that the d₇₅ value of the ink containing thecoloring material falls within the above range, the ink is found tosuppress the occurrence of the bronze phenomenon and have highenvironmental gas resistance.

A molecular density in a solution must be kept constant in order tomeasure the d value by a small-angle X-ray scattering method. Therefore,the d value is preferably measured by using ink with its coloringmaterial concentration kept constant. In the present invention, ascattering angle profile was measured by using ink prepared in such amanner that the coloring material content (mass %) would be 0.5 mass %with respect to the total mass of the ink. When ink had a coloringmaterial content in excess of 0.5 mass %, the ink was diluted with purewater to have a coloring material concentration of 0.5 mass %, and thescattering angle profile of the diluted ink was measured. The fact thatink has a coloring material content of 0.5 mass % can be examined on thebasis of the fact that the absorbance measured after diluting 150 timesthe ink with pure water is in the range of 1.15 to 1.30. The conditionsunder which the absorbance is measured are as follows.

Spectrophotometer: Self-recording spectrophotometer (trade name: U-3300;manufactured by Hitachi, Ltd.)

Measurement cell: 1 cm quartz cell

Sampling interval: 0.1 nm

Scanning rate: 30 nm/min

Number of measurements: Measurement is performed five times to take theaverage value of the five measurements.

The aggregation properties of a coloring material described above has acorrelation also with the maximum absorption wavelength (λmax) in anabsorption spectrum. Ink having higher molecular aggregation properties(a higher d₇₅ value) tends to have smaller λmax. Therefore, a coloringmaterial can be evaluated for its aggregation properties by means ofλmax having a correlation with the d₇₅ value. In this case, it has beenfound that ink effectively suppresses the occurrence of the bronzephenomenon and has high environmental gas resistance when λmax in theink diluted 2,000 times with pure water is 608.0 nm or more and 613.0 nmor less. It has also been found that ink particularly effectivelysuppresses the occurrence of the bronze phenomenon and has highenvironmental gas resistance when the λmax is 610.0 nm or more and 613.0nm or less. In other words, in the case where the aggregation propertiesof the compound represented by the general formula (I) or the saltthereof as a coloring material is controlled in such a manner that theλmax of the ink containing the coloring material falls within the aboverange, the ink is found to suppress the occurrence of the bronzephenomenon and have high environmental gas resistance. The conditionsunder which the maximum absorption wavelength is measured are the sameas the above-described conditions under which the absorbance ismeasured.

The coloring material used in the present invention is known to be lesslikely to aggregate when it has a smaller number of unsubstitutedsulfamoyl groups and a larger number of substituted sulfamoyl groups orof sulfonic groups. In particular, in the case where a coloring materialsatisfies the requirement concerning the d₇₅ value in the presentinvention, the coloring material preferably contains a compound in whichthe number of substituents 1≧1 in the compound represented by thegeneral formula (I) or the salt thereof, or in the compound representedby the general formula (II) or the salt thereof because the aggregationof the coloring material can be suppressed.

[Method of Testing Coloring Material]

Exemplified Compound 1 (the compound represented by the general formula(II) or the salt thereof), which is an example of the coloring materialused in the present-invention, can be tested by the following methods(1) to (3) each of which involves the use of high performance liquidchromatography (HPLC).

-   (1) Retention time of the peak-   (2) Maximum absorption wavelength in the peak of (1)-   (3) M/Z (posi) of mass spectrum in the peak of (1)

Analysis conditions for high performance liquid chromatography are asshown below. An ink solution diluted 50 times with pure water isanalyzed by means of high performance liquid chromatography under thefollowing conditions to measure the retention time of a main peak andthe maximum absorption wavelength of a peak.

Column: Symmetry C18 2.1 mm×150 mm

Column temperature: 40° C.

Flow rate: 0.2 ml/min

PDA: 210 nm to 700 nm

Mobile phase and gradient condition: Table 3

TABLE 3 0–15 min 15–30 min A Water 87.5% → 0%       0% B Acetonitrile10% → 97.5% 97.5% C 200-mmol/l aqueous solution 2.5%  2.5% of ammoniumacetate

In addition, analysis conditions for a mass spectrum are as shown below.The mass spectrum of the resultant peak is measured under the followingconditions, and the M/Z (posi) is measured.

Ionization Method

ESI Capillary voltage 3.1 kV Desolvating gas 300° C. Ion sourcetemperature 120° C.

Detector posi 40 V 500-2,000 amu/0.9 sec

Table 4 shows the values of the retention time, maximum absorptionwavelength, and M/Z of Exemplified Compound 1. When a coloring materialhas values shown in Table 4, the coloring material can be judged to beusable in the present invention. In the coloring material used in thepresent invention, the peak ratio of the mass spectrum obtained from apeak of high performance liquid chromatography (HPLC) varies dependingon a mixing ratio of isomers different from each other in the number,kinds, and substitution positions of substituents in the coloringmaterial, but the peak of the M/Z described in Table 4 below ischaracterized in that it is always detected. Therefore, the presentmethod of testing a coloring material is effective in examining whetherink contains the coloring material used in the present invention.

TABLE 4 Maximum absorption Retention time wavelength [min] [nm]M/Z(Posi) 6.9–7.2 600–620 1670–1672

(Aqueous Medium)

An ink composition of the present invention can use water or an aqueousmedium which is a mixed solvent of water and any one of variouswater-soluble organic solvents.

There is no particular limitation concerning the water-soluble organicsolvent as long as they are water-soluble, and preferable examplesthereof include: an alkyl alcohol having 1 to 4 carbon atoms such asethanol, isopropanol, n-butanol, isobutanol, 2-butanol, or 3-butanol; acarboxylic acid amide such as N,N-dimethylformamide orN,N-dimethylacetamide; a ketone or a keto alcohol such as acetone,methyl ethyl ketone, or 2-methyl-2-hydroxypentan-4-one; a cyclic ethersuch as tetrahydrofuran or dioxane; a polyhydric alcohol such asglycerin, ethylene glycol, diethylene glycol, triethylene glycol,tetraethylene glycol, 1,2 or 1,3-propylene glycol, 1,2 or 1,4-butyleneglycol, polyethylene glycol, 1,3-butanediol, 1,5-pentanediol,1,2-hexanediol, 1,6-hexanediol, dithioglycol, 2-methyl-1,3-propanediol,1,2,6-hexanetriol, an acetylene glycol derivative, ortrimethylolpropane; an alkyl ether of a polyhydric alcohol such asethylene glycol monomethyl (or ethyl) ether, diethylene glycolmonomethyl (or ethyl) ether, or triethylene glycol monoethyl (or butyl)ether; a heterocyclic compound such as 2-pyrrolidone,N-methyl-2-pyrrolidone, 1,3-dimethyl-2-imidazolidinone, orN-methylmorpholine; a sulfur-containing compound such as dimethylsulfoxide; and urea and a urea derivative. Each of those water-solubleorganic solvents may be used alone, or two or more of them may be usedas a mixture.

The content of such a water-soluble organic solvent is preferably 5.0mass % to 90.0 mass %, or more preferably 10.0 mass % to 50.0 mass %with respect to the total mass of ink. The reason therefore is asfollows. If the content is smaller than the range, reliability forejection properties., etc. may lower when the water-soluble organicsolvent is used for ink jet ink, on the other hand, if the content islarger than the range, insufficient ink supply due to an increase inviscosity of ink may occur.

Deionized water (ion-exchange water) is preferably used as water. Thewater content is preferably 10.0 mass % to 90.0 mass % with respect tothe total mass of ink.

In the present invention, among the above-described water-solubleorganic solvents, 2-pyrrolidone is preferable because it is particularlyeffective in suppressing the occurrence of the bronze phenomenon when itis used in combination with the compound represented by the generalformula (I) or the salt thereof. The content (mass %) of 2-pyrrolidonein ink is preferably 50.0% or more with respect to the coloring materialcontent (mass %) in order to obtain the effect by incorporating2-pyrrolidone into the ink.

Examples of a water-soluble organic solvent having the same effect as2-pyrrlidone include a polyethylene glycol (having a molecular weight of200 or more) and an alkyl ether of a polyhydric alcohol such astriethylene glycol monoethyl ether.

The mechanism for suppressing the occurrence of the bronze phenomenon bythose specific water-soluble organic solvents is unclear, but isestimated to be as follows. The d₇₅ value of ink obtained by asmall-angle X-ray scattering method does not change depending on thepresence or absence of those specific water-soluble organic solvents inthe ink. In view of this, those specific water-soluble organic solventsdo not change the aggregation properties of a coloring material in theink, and are capable of suppressing the aggregation of molecularaggregates of the coloring material on the recording medium. The content(mass %) of those specific water-soluble organic solvents in ink ispreferably 50.0% or more with respect to the coloring material content(mass %) in order for the effect to be exhibited by incorporating thosespecific water-soluble organic solvents into the ink.

(Other Additive)

In addition, in the present invention, various additives such as asurfactant, a pH adjustor, a rust inhibitor, an antiseptic, amildewproofing agent, a chelating agent, a UV absorber, a viscositymodifier, a defoaming agent, and a water-soluble polymer may beincorporated as required.

Specific examples of the surfactant include an anionic surfactant, anampholytic surfactant, a cationic surfactant, and a nonionic surfactant.

Specific examples of the anionic surfactant include: an alkylsulfocarboxylate; an α-olefin sulfonate; a polyoxyethylene alkyl etheracetate; N-acylamino acid or a salt thereof; an N-acylmethyltaurinesalt; an alkyl sulfonate polyoxyalkyl ether sulfonate; an alkylsulfonate polyoxyethylene alkyl ether phosphate; resin acid soap; acastor oil sulfonate; lauryl alcohol sulfonate; an alkyl phenolphosphate; an alkyl phosphate; an alkyl allyl sulfonate; a diethylsulfosuccinate; and a diethyl hexyl sulfosuccinate dioctylsulfosuccinate.

Specific examples of the cationic surfactant include a 2-vinylpyridinederivative and a poly4-vinylpyridine derivative. Examples of theampholytic surfactant include lauryl dimethyl aminoacetic acid betaine,2-alkyl-N-carboxymethyl-N-hydroxyethylimidazolinium betaine, coconut oilfatty amide propyl dimethyl aminoacetic acid betaine, polyoctylpolyamino ethyl glycin, and other imidazoline derivatives.

Specific examples of the nonionic surfactant include: ethers such aspolyoxyethylene nonyl phenyl ether, polyoxyethylene octyl phenyl ether,polyoxyethylene dodecyl phenyl ether, polyoxyethylene lauryl ether,polyoxyethylene oleyl ether, polyoxyethylene alkyl ether, andpolyoxyaralkyl alkyl ether; esters such as polyoxyethylene oleic acid,polyoxyethylene oleate, polyoxyethylene distearate, sorbitan laurate,sorbitan monostearate, sorbitan monooleate, sorbitan sesquioleate,polyoxyethylene monooleate, and polyoxyethylene stearate; and acetyleneglycol-based nonionic surfactants such as2,4,7,9-tetramethyl-5-decyne-4,7-diol, 3,6-dimethyl-4-octyne-3,6-diol,and 3,5-dimethyl-1-hexyen-3-ol (for example, Acetylenol EH manufacturedby Kawaken Fine Chemicals Co., Ltd. and Surfynol 104, 82, and 465, andOlfin STG manufactured by Nissin Chemical Industry Co., Ltd.).

Any substance can be used as a pH adjustor as long as the substance iscapable of adjusting the pH of ink to fall within the range of 6.0 to11.0. Examples of such substance include: alcoholamine compounds such asdiethanolamine, triethanolamine, isopropanolamine, andtrishydroxymethylaminomethane; hydroxides of alkali metals such aslithium hydroxide and potassium hydroxide; ammonium hydroxide; andcarbonates of alkali metals such as lithium carbonate, sodium carbonate,and potassium carbonate. Of those, alcoholamine compounds such asdiethanolamine, triethanolamine, isopropanolamine, andtrishydroxymethylaminomethane, and carbonates of alkali metals such aslithium carbonate, sodium carbonate, and potassium carbonate arepreferable because each of them has a suppressing effect on theoccurrence of the bronze phenomenon.

Specific examples of the antiseptic and the mildewproofing agent includeorganic sulfur-based, organic nitrogen sulfur-based, organichalogen-based, haloallylsulfone-based, iodopropagil-based,N-haloalkylthio-based, benzothiazole-based, nithochirile-based,pyridine-based, 8-oxyquinoline-based, benzothiazole-based,isothiazoline-based, dithiol-based, pyridine oxide-based,nitropropane-based, organotin-based, phenol-based, quaternary ammoniumsalt-based, triazine-based, thiadiazine-based, anilide-based,adamantane-based, dithiocarbamate-based, brominated indanone-based,benzyl bromoacetate-based, and inorganic salt-based compounds.

An example of the organic halogen-based compound includespentachlorophenol sodium. An example of the pyridine oxide-basedcompound includes 2-pyridinethiol-loxide sodium. An example of theinorganic salt-based compound includes soda acetic anhydride. Examplesof the isothiazoline-based compound include:1,2-benzoisothiazolin-3-one, 2-n-octyl-4-isothiazolin-3-one,5-chloro-2-methyl-4-isothiazolin-3-one,5-chloro-2-methyl-4-isothiazolin-3-one magnesium chloride, and5-chloro-2-methyl-4-isothiazolin-3-one calcium chloride. Other specificexamples of the antiseptic and the mildewproofing agent include sodasorbate sodium benzoate such as Proxel GXL (S) and Proxel XL-2 (S)manufactured by Avecia.

Examples of the chelating agent include sodium citrate, sodiumethylenediamine tetraacetate, sodium dinitrotriacetate, sodiumhydroxyethylethylenediamine triacetate, sodium diethylenetriaminepentaacetate, and sodium uramil diacetate.

Examples of the rust inhibitor include an acid sulfite, sodiumthiosulfate, ammonium thioglycolate, diisopropylammonium nitrite,pentaerythritol tetranitrate, and dicyclohexylammonium nitrite.

Examples of the UV absorber include a benzophenone-based compound, abenzotriazole-based compound, a cinnamic acid-based compound, atriazine-based compound, a stilbene-based compound, or compounds thatabsorb ultraviolet light to emit fluorescence typified by abenzoxazole-based compound, so-called fluorescent whitening agents.

Examples of the viscosity modifier include water-soluble polymercompounds in addition to water-soluble organic solvents, and examples ofthe water-soluble polymer compounds include polyvinyl alcohol, acellulose derivative, polyamine, and polyimine.

A fluorine-based or silicone-based compound is used as the defoamingagent as required.

<Recording Medium>

Any recording medium can be used for forming images by means of the inkof the present invention as long as recording is performed by applyingthe ink to the recording medium.

The present invention is applicable to a recording medium in which acoloring material such as a pigment is adsorbed to fine particlesforming a porous structure in an ink-receiving layer and an image isformed from at least the fine particles with the coloring materialadsorbed thereto, and is particularly suitable for the case where an inkjet method is used. Such an ink jet recording medium is preferably of aso-called absorption type in which ink is absorbed by a gap formed in anink-receiving layer on a support.

An absorption type ink-receiving layer is constituted as a porous layermainly composed of fine particles and containing a binder and any otheradditive as required. Specific examples of the fine particles include:inorganic pigments such as silica, clay, talc, calcium carbonate,kaolin, aluminum oxide (for example, alumina or alumina hydrate),diatomaceous earth, titanium oxide, hydrotalcite, and zinc oxide; andorganic pigments such as a urea formalin resin, an ethylene resin, and astyrene resin. One or more kinds of them may be used. Examples of abinder that is suitably used include a water-soluble polymer and latex.For example, the following may be cited: polyvinyl alcohol or a modifiedproduct thereof; starch or a modified product thereof; gelatin or amodified product thereof; gum arabic; cellulose derivatives such ascarboxymethylcellulose, hydroxyethylcellulose, andhydroxyproylmethylcellulose; vinyl-based copolymer latexes such as anSBR latex, an NBR latex, a methyl methacrylate-butadiene copolymerlatex, a functional group-denatured polymer latex, and an ethylene-vinylacetate copolymer; polyvinyl pyrrolidone; maleic anhydride or acopolymer thereof; and an acrylate copolymer. Two or more kinds of themmay be used in combination as required. In addition, an additive may beused, and examples of an additive to be used as required include adispersant, a thickener, a pH adjustor, a lubricant, a fluiditydenaturing agent, a surfactant, a defoaming agent, a releasing agent, afluorescent bleach, a UV absorber, and an antioxidant.

In particular, a recording medium having an ink-receiving layer formedthereon which is mainly composed of fine particles having an averageparticle size of 1 μm or less is preferably used in the presentinvention. Specific examples of the fine particles include silica fineparticles and aluminum oxide fine particles. Preferable silica fineparticles are silica fine particles typified by colloidal silica.Colloidal silica, which itself is available in the market, isparticularly preferably what is described in JP 2803134 B or JP 2881847B. Preferable aluminum oxide fine particles are alumina hydrate fineparticles and the like. An alumina hydrate represented by the followinggeneral formula may be exemplified as one example of such aluminahydrate fine particles.Al₂O_(3-n)(OH)_(2n)._(m)H₂O(In the formula, n represents an integer of 1, 2, or 3, and m representsa value of 0 to 10, or preferably 0 to 5; provided, however, that m andn are not simultaneously 0. m may be or may not be an integer becausemH₂O also represents an aqueous phase that can desorb and is notinvolved in the formation of an mH₂O crystal lattice in many cases. Inaddition, when heating such kind of material, m may reach 0.)

An alumina hydrate can be produced by a conventionally known method suchas: the hydrolysis of aluminum alkoxide or sodium aluminate described inU.S. Pat. No. 4,242,271 or U.S. Pat. No. 4,202,870; or a methodinvolving adding an aqueous solution of sodium sulfate, aluminumchloride, or the like to an aqueous solution of sodium aluminate or thelike to perform neutralization described in JP 57-44605 B.

The recording medium preferably has a support for supporting theabove-described ink-receiving layer. Any support may be use without anyparticular limitation as long as its ink-receiving layer can be formedof the above-described porous fine particles and it provides rigiditywhich enables it to be conveyed by a conveying mechanism of an ink jetprinter or the like. Specific examples thereof include: a paper supportformed of a pulp raw material mainly composed of natural cellulosefibers; a plastic support composed of a material such as polyester (forexample, polyethylene terephthalate), cellulose triacetate,polycarbonate, polyvinyl chloride, polypropylene, or polyimide;resin-coated paper (for example, RC paper) having, on at least one sideof base paper, a polyolefin resin coating layer in which a white pigmentor the like is added.

<Ink Jet Recording Method>

The ink according to the present invention is particularly suitably usedfor an ink jet recording method including the step of ejecting the inkby an ink jet method. Examples of the ink jet recording method include arecording method involving applying mechanical energy to ink to ejectthe ink and a recording method involving applying thermal energy to inkto eject the ink. An ink jet recording method involving the use ofthermal energy is particularly preferably used in the present invention.

<Ink Cartridge>

An example of an ink cartridge suitable for performing recording byusing the ink according to the present invention includes an inkcartridge including an ink storage portion for storing the ink.

<Recording Unit>

An example of a recording unit suitable for performing recording byusing the ink according to the present invention includes a-recordingunit including an ink storage portion for storing the ink and arecording head. In particular, a recording unit in which the recordinghead applies thermal energy corresponding to a recording signal to theink to generate an ink droplet by virtue of the energy can beexemplified.

<Ink Jet Recording Apparatus>

An example of a recording apparatus suitable for performing recording byusing the ink according to the present invention includes a recordingapparatus in which thermal energy corresponding to a recording signal isapplied to ink in the chamber of a recording head having an ink storageportion for storing the ink to generate an ink droplet by virtue of theenergy.

The schematic constitution of a mechanism portion of an ink jetrecording apparatus will be described below. A recording apparatus mainbody is constituted of a sheet feeding portion, a sheet conveyingportion, a carriage portion, a sheet discharge portion, and a cleaningportion, and an external packaging portion for protecting them andproviding them with a design, each of which plays a role of eachmechanism. The outline of each of them will be described below.

FIG. 4 is a perspective view of a recording apparatus. FIGS. 5 and 6 areviews for explaining the internal mechanism of a recording apparatusmain body. FIG. 5 is a perspective view seen from an upper rightportion, and FIG. 6 is a side sectional view of the recording apparatusmain body.

When sheets are fed in the recording apparatus, only the predeterminednumber of recording media are sent to a nip portion composed of a sheetfeeding roller M2080 and a separating roller M2041 in the sheet feedingportion including a sheet feeding tray M2060. The sent recording mediaare separated at the nip portion, and only the uppermost recordingmedium is conveyed. The recording medium sent to the sheet conveyingportion is guided by a pinch roller holder M3000 and a paper guideflapper M3030 to be sent to a roller pair composed of a conveying rollerM3060 and a pinch roller M3070. The roller pair composed of theconveying roller M3060 and the pinch roller M3070 are driven and rotatedby an LF motor E0002, whereby the recording medium is conveyed through aplaten M3040.

In the carriage portion, when an image is formed on a recording medium,a recording head H1001 (FIG. 7) is arranged at a target image formingposition, and ink is ejected to the recording medium in accordance witha signal from an electrical substrate E0014. Details about theconstitution of the recording head H1001 will be described later. Whilerecording is performed by the recording head H1001, recording mainscanning in which a carriage M4000 scans in the column direction and subscanning in which a recording medium is conveyed in the row direction bythe conveying roller M3060 are alternately repeated, whereby an image isformed on the recording medium.

Finally, the recording medium on which an image has been formed ispinched at a nip between a first sheet discharge roller M3110 and a spurM3120 in the sheet discharge portion, conveyed, and discharged to asheet discharge tray M3160.

In the cleaning portion, when a pump M5000 is allowed to act in such astate that a cap M5010 is brought into close contact with an inkejection port of the recording head H1001 for the purpose of cleaningthe recording head H1001 before and after image recording, unnecessaryink and the like are sucked from the recording head H1001. The inkremaining in the cap M5010 is sucked with the cap M5010 opened, wherebyneither adhesion of the remaining ink nor a subsequent harmful effectoccurs.

(Constitution of Recording Head)

The constitution of a head cartridge H1000 will be described below. Thehead cartridge H1000 includes the recording head H1001, means formounting ink tanks H1900, and means for supplying ink from the ink tanksH1900 to the recording head, and is detachably mounted on the carriageM4000.

FIG. 7 shows how the ink tanks H1900 are mounted on the head cartridgeH1000. The recording apparatus forms images by means of yellow, magenta,cyan, black, pale magenta, pale cyan, and green inks, and so the inktanks H1900 are independently prepared for seven colors. The inkaccording to the present invention is used for at least one of the aboveinks. In addition, as shown in the figure, each ink tank is detachableto the head cartridge H1000. The ink tanks H1900 can be detached in sucha state that the head cartridge H1000 is mounted on the carriage M4000.

FIG. 8 shows an exploded perspective view of the head cartridge H1000.In the figure, the head cartridge H1000 includes a first recordingelement substrate H1100, a second recording element substrate H1001, afirst plate H1200, a second plate H1400, an electric wiring substrateH1300, a tank holder H1500, a flow path forming member H1600, a filterH1700, and a seal rubber H1800.

Each of the first recording element substrate H1100 and the secondrecording element substrate H1101 is a Si substrate having multiplerecording elements (nozzles) for ejecting ink formed on one side bymeans of photolithography. Electric wiring made of Al or the like forsupplying power to each recording element is formed by means of a filmformation technique, and multiple ink flow paths corresponding to theindividual recording elements are also formed by means ofphotolithography. Furthermore, ink supply ports for supplying ink to themultiple ink flow paths are formed so as to open on the rear surface.

FIG. 9 is an enlarged front view for explaining the constitution of eachof the first recording element substrate H1100 and the second recordingelement substrate H1101. Reference symbols H2000 to H2600 denoterecording element trains (hereinafter referred to also as nozzle trains)corresponding to different ink colors. The first recording elementsubstrate H1100 has nozzle trains for three colors: the nozzle trainH2000 to which yellow ink is supplied, the nozzle train H2100 to whichmagenta ink is supplied, and the nozzle train H2200 to which cyan ink issupplied. The second recording element substrate H1101 has nozzle trainsfor four colors: the nozzle train H2300 to which pale cyan ink issupplied, the nozzle train H2400 to which black ink is supplied, thenozzle train H2500 to which orange ink is supplied, and the nozzle trainH2600 to which pale magenta ink is supplied.

Each nozzle train is constituted by 768 nozzles arranged at intervals of1,200 dpi (dot/inch; reference value) in the conveying direction of arecording medium, and each nozzle ejects about 2 pl of ink. An openingarea in each nozzle ejection port is set to be about 100 μm². The firstrecording element substrate H1100 and the second recording elementsubstrate H1101 are bonded and fixed to the first plate H1200 having inksupply ports H1201 formed thereon for supplying ink to the firstrecording element substrate H1100 and the second recording elementsubstrate H1101.

The second plate H1400 having openings is also bonded and fixed to thefirst plate H1200. The second plate H1400 holds the electric wiringsubstrate H1300 in such a manner that the electric wiring substrateH1300, the first recording element substrate H1100, and the secondrecording element substrate H1101 are electrically connected.

The electric wiring substrate H1300 impresses electrical signals forcausing each of the nozzles formed on the first recording elementsubstrate H1100 and the second recording element substrate H1101 toeject ink. The electric wiring substrate H1300 has: electric wiringcorresponding to each of the first recording element substrate H1100 andthe second recording element substrate H1101; and an external signalinput terminal H1301 which is positioned at the end portion of theelectric wiring to receive electrical signals from the recordingapparatus main body. The external signal input terminal H1301 ispositioned and fixed to the back surface side of the tank holder H1500.

The flow path forming member H1600 is fixed by means of, for example,ultrasonic welding to the tank holder H1500 for holding the ink tanksH1900. Thus, an ink flow path H1501 passing from the ink tanks H1900 tothe first plate H1200 is formed.

The filter H1700 is arranged at the end portion on the ink tank side ofthe ink flow path H1501 engaged with the ink tanks H1900, and so thefilter H1700 prevents dust from entering from the outside. The sealrubber H1800 is mounted on the portion at which the ink flow path H1101is engaged with the ink tanks H1900 to prevent ink from evaporating fromthe portion.

Furthermore, as described above, the head cartridge H1000 is made up byconnecting a tank holder portion constituted of the tank holder H1500,the flow path forming member H1600, the filter H1700 and the seal rubberH1800, with the recording head portion H1001 constituted of the firstrecording element substrate H1100, the second recording elementsubstrate H1101, the first plate H1200, the electric wiring substrateH1300 and the second plate H1400 by the use of an adhesive or the like.

Description has been made here by taking, as an example of an embodimentof a recording head, a recording head according to a bubble jet(registered trademark) method that performs recording by means of anelectrothermal converter (recording element) for generating thermalenergy for causing ink to generate film boiling in accordance with anelectrical signal.

As for the representative structure and principle, it is preferred touse basic principles disclosed in, for example, U.S. Pat. No. 4,723,129and U.S. Pat. No. 4,740,796. The method is applicable to any one of aso-called on-demand type and a so-called continuous type. In particular,the method is effective for the on-demand type because of the followingreason. At least one driving signal which corresponds to recordinginformation and causes a sudden increase in temperature exceedingnuclear boiling is applied to electrothermal converters arrangedcorresponding to a sheet or liquid flow path holding a liquid (ink),thereby causing the electrothermal converter to generate thermal energy.Then, film boiling is generated on the thermal action surface of arecording head. As a result, an air bubble in the liquid (ink) can beformed so as to be in one-to-one correspondence with the driving signal.The growth and contraction of the air bubble eject the liquid (ink)through an opening for ejection, thereby forming at least one droplet.It is more preferable that the driving signal is of a pulse shapebecause the growth and contraction of an air bubble can be performedimmediately and appropriately, and hence the liquid (ink) can be ejectedwith excellent responsiveness.

As an example of a second embodiment of an ink jet recording apparatusutilizing mechanical energy, an on-demand ink jet recording head may becited, including: a nozzle forming substrate having multiple nozzles;pressure generating means arranged so as to be opposite to the nozzlesand composed of a piezoelectric material and a conductive material; andink filling the surroundings of the pressure generating means, in whichthe pressure generating means is displaced by an applied voltage toeject a small ink droplet from a nozzle.

The ink jet recording apparatus is not limited to such apparatuses asdescribed above in which a head and an ink tank are separated, and maybe one in which a head and an ink tank are unified so that they areunseparable. The ink tank may be separably or unseparably unified withthe head to be mounted on a carriage, or may be mounted at a fixingportion of an apparatus to supply ink to a recording head through an inksupply member such as a tube. When the ink tank is provided with aconstitution for applying a suitable negative pressure to the recordinghead, an absorber may be arranged in an ink storage portion of the inktank, or the ink tank may have a flexible ink storage bag and a springportion for applying bias in the direction of expanding the internalvolume of the bag. The recording apparatus may adopt a serial recordingmethod as described above, or may be in the form of a line printerobtained by aligning recording elements over the range corresponding tothe entire width of a recording medium.

EXAMPLES

Hereinafter, the present invention will be described in more detail byway of examples and comparative examples. However, the present inventionis not limited to the following examples unless the examples depart fromthe gist of the present invention. Unless otherwise specified, the term“part” of each ink component in examples and comparative examplesrepresents “part by mass”.

<Synthesis of Coloring Material>

(1) Synthesis of Tetrasodium Copper Phthalocyanine Tetrasulfonate(Compound (2))

Sulfolane, monosodium 4-sulfophthalate, ammonium chloride, urea,ammonium molybdate, and copper(II) chloride were mixed, stirred, andwashed with methanol. After that, water was added to the resultantproduct, and an aqueous solution of sodium hydroxide was used to adjustthe pH of the solution to 11. An aqueous solution of hydrochloric acidwas added to the resultant solution under stirring, and then sodiumchloride was gradually added to separate out crystals. The resultantcrystals was filtered out and washed with a 20% aqueous solution ofsodium chloride, and then methanol was added. The separated out crystalswere filtered out, washed with a 70% aqueous solution of methanol, anddried to yield tetrasodium copper phthalocyanine tetrasulfonate(Compound (2)) as blue crystals.

(2) Synthesis of Copper Phthalocyanine Tetrasulfonic Chloride (Compound(3))

Tetrasodium copper phthalocyanine tetrasulfonate (Compound (2)) thusprepared was gradually added to chlorosulfonic acid, and then thionylchloride was added dropwise to perform reaction. After that, thereaction solution was cooled, and the precipitated crystal was filteredto yield a wet cake of copper phthalocyanine tetrasulfonic chloride.

(3) Synthesis of the Following Compound (4)

A compound (4) is a compound represented by the general formula (IV)wherein Y represents an amino group and R₁ and R₂ each represent asulfonic group substituted at the 2 or 5 position.

Lipal OH, cyanuric chloride, and monosodium aniline-2,5-disulfonate wereadded in an ice water, and was allowed to react while an aqueoussolution of sodium hydroxide was added. Next, an aqueous solution ofsodium hydroxide was added to the reaction solution to adjust the pH ofthe reaction solution to 10. 28% ammonia water and ethylenediamine wereadded to the reaction solution to perform reaction. Sodium chloride andconcentrated hydrochloric acid were added to the resultant reactionsolution to separated out crystals. The separated out crystals werefiltered and fractionated, and was washed with a 20% aqueous solution ofsodium chloride to prepare a wet cake. Methanol and water were added tothe resultant wet cake, and the whole was filtered, washed withmethanol, and dried to yield the compound (4).

(4) Synthesis of Coloring Materials A to G

The wet cake of copper phthalocyanine tetrasulfonic chloride (Compound(3)) synthesized in the above (2) was added to an ice water, and thewhole was stirred to prepare a suspension. Ammonia water and thecompound (4) synthesized in (3) were added to the suspension to performreaction. Water and sodium chloride were added to the mixture toseparate out crystals. The resultant crystals was filtered, washed withan aqueous solution of sodium chloride, and filtered again, washed, anddried to yield a coloring material A as blue crystals. In view of theabove reaction, the compound is estimated to be a coloring materialwhich is a compound represented by Exemplified Compound 1 and hasaverage numbers of substituents in the general formula (I) of 1=1.0 to1.5, m=1.5 to 2.0, and n=2.0 to 2.5.

Coloring materials B to G which were compounds each represented byExemplified Compound 1 and were different from one another in theaverage number of substituents in the general formula (I) weresynthesized in the same synthesis procedure as described above. Table 5below shows the average number of substituents in each of the coloringmaterials A to G.

TABLE 5 Coloring material l m n A 1.0–1.5 1.5–2.0 2.0–2.5 B 0 1.5–2.51.5–2.5 C 1.0–1.5 1.0–1.5 2.0–2.5 D 0 1.5–2.5 1.5–2.5 E 1.0–1.5 1.0–1.52.0–2.5 F 0 2.5–3.0 0.5–1.0 G   0–1.0 1.0–1.5 2.0–2.5

<Evaluation of Bronze Resistance>

(1) Preparation of Ink

The respective components shown in Table 6 below were mixed andsufficiently stirred. After that, the resultant product was filteredthrough a membrane filter having a pore size of 0.2 μm under pressure toprepare each of inks A to D.

TABLE 6 Ink A B C D Coloring material A 0.5 Coloring material B 0.5Coloring material C 0.5 Coloring material D 0.5 Glycerin 20.0 20.0 20.020.0 2-pyrrolidone 2.5 2.5 2.5 2.5 Acetylenol EH (*) 1.0 1.0 1.0 1.0Ion-exchanged water 76.0 76.0 76.0 76.0 (*) Ethylene oxide adduct ofacetylene glycol (surfactant; manufactured by Kawaken Fine ChemicalsCo., Ltd.)

(2) Measurement of d₇₅ Value

The scattering angle profile of each of the inks A to D (each having acoloring material concentration of 0.5 mass %) was measured by means ofa small-angle X-ray scattering method. The scattering angle profile wasmeasured under the following conditions.

Apparatus: Nano Viewer (manufactured by Rigaku)

X-ray source: Cu—Kα

Output: 45 kV-60 mA

Effective focal spot: 0.3 mmΦ+Confocal Max−Flux Mirror

1^(st) Slit: 0.5 mm, 2^(nd) Slit: 0.4 mm, 3^(rd) Slit: 0.8 mm

Irradiation time: 240 min

Beam stopper: 3.0 mmΦ

Measurement method: Penetration method

Detector: Blue Imaging Plate

A peak area obtained by removing a background and a 2θ value accountingfor 75% or more of the entire peak area (2θ₇₅ value) were measured fromthe resultant scattering angle profile by means of an X-ray diffractiondata processing soft JADE (Material Data, Inc.). The d₇₅ value wascalculated from the 2θ₇₅ value on the basis of the following expression(2). Table 7 shows the results.d ₇₅=λ/2 sin θ₇₅  Eq. (2)

(3) Measurement of Maximum Absorption Wavelength (λmax)

After each of the inks A to D (each having a coloring materialconcentration of 0.5 mass %) had been diluted 2,000 times with purewater, the maximum absorption wavelength (λmax) was measured. Table 7shows the results. The maximum absorption wavelength (λmax) was measuredunder the following conditions.

Spectrophotometer: Self-recording spectrophotometer (trade name: U-3300;manufactured by Hitachi, Ltd.)

Measurement cell: 1 cm quartz cell

Sampling interval: 0.1 nm

Scanning rate: 30 nm/min

Number of measurements: Measurement was performed five times to take theaverage value of the five measurements.

(4) Creation of Recorded Product

Each of the inks A to D thus prepared was mounted on an ink jetrecording apparatus (trade name: Pixus 950i; manufactured by CANON Inc.)to print a 13-level gradation pattern on an ink jet glossy medium (tradename: PR101; manufactured by CANON Inc.) by changing a printing duty to5, 12, 21, 29, 35, 43, 51, 58, 66, 74, 85, 90, and 100%. Thus, arecorded product was created.

(5) Evaluation of Bronze Resistance

The printing duty at which the bronze phenomenon occurred in the13-level gradation pattern of the recorded product thus created wasvisually observed to define the printing duty as the printing duty atwhich the bronze phenomenon occurred. In general, the bronze phenomenonis apt to occur with increasing the printing duty. In other words, thebronze phenomenon is more likely to occur where the ink has a lowerprinting duty at which the bronze phenomenon occurs, while the bronzephenomenon is less likely to occur where the ink has a higher printingduty at which the bronze phenomenon occurs. The criteria for the bronzeresistance are as follows. Table 7 shows the results of the evaluation.

-   A: The printing duty at which the bronze phenomenon occurs is 55% or    more.-   B: The printing duty at which the bronze phenomenon occurs is 40% or    more and less than 55%.-   C: The printing duty at which the bronze phenomenon occurs is less    than 40%.

TABLE 7 d₇₅ Maximum absorption value wavelength Bronze Ink [nm] λmax[nm] resistance Example A 7.52 612 A B 10.59 608.1 B C 6.71 612.9 AComparative D 10.61 607.9 C Example

<Evaluation of Bronze Resistance and Environmental Gas Resistance>

(1) Preparation of Ink

The respective components were mixed according to each of theformulations 1 to 4 shown in Table 8 below and sufficiently stirred.After that, the resultant product was filtered through a membrane filterhaving a pore size of 0.2 μm under pressure to prepare ink. The inksprepared by using the coloring material A according to the formulations1 to 4 were denoted by A1 to A4, and the inks prepared by using thecoloring material B according to the formulations 1 to 4 were denoted byB1 to B4 (the same holds true for the other inks). Thus, a total of 28kinds of inks A1 to G4 were prepared.

TABLE 8 For- For- mulation 1 Formulation 2 Formulation 3 mulation 4Coloring 1.5 1.5 1.5 1.5 material Glycerin 10.0 10.0 10.0 10.0 Ethylene8.0 8.0 8.0 8.0 glycol 2- 2.5 0.8 0.7 pyrrolidone Diethylene 1.7 1.8 2.5glycol Acetylenol 0.8 0.8 0.8 0.8 EH (*) Ion- 77.2 77.2 77.2 77.2exchanged water (*) Ethylene oxide adduct of acetylene glycol(surfactant; manufactured by Kawaken Fine Chemicals Co., Ltd.)

(2) Measurement of d₇₅ Value

The scattering angle profile of each of the inks A1 to G4 was measuredby means of a small-angle X-ray scattering method, provided that each ofthe inks was diluted 3 times with pure water before the scattering angleprofile of the ink was measured by the means of small-angle X-rayscattering method.

The scattering angle profile was measured under the followingconditions.

Apparatus: Nano Viewer (manufactured by Rigaku)

X-ray source: Cu—Kα

Output: 45 kV-60 mA

Effective focal spot: 0.3 mmΦ+Confocal Max−Flux Mirror

1^(st)st Slit: 0.5 mm, 2^(nd) Slit: 0.4 mm, 3^(rd) Slit: 0.8 mm

Irradiation time: 40 min

Beam stopper: 3.0 mmΦ

Measurement method: Penetration method

Detector: Blue Imaging Plate

A peak area obtained by removing a background and a 2θ value accountingfor 75% or more of the entire peak area (2θ₇₅ value) were measured fromthe resultant scattering angle profile by means of an X-ray diffractiondata processing soft JADE (Material Data, Inc.). The d₇₅ value wascalculated from the 2θ₇₅ value on the basis of the following expression(2). Table 9 shows the results.d ₇₅=λ/2 sin θ₇₅  Eq. (2)

(3) Measurement of Maximum Absorption Wavelength (λmax)

After each of the inks A1 to G4 (each having a coloring materialconcentration of 1.5 mass %) had been diluted 2,000 times with purewater, the maximum absorption wavelength (λmax) was measured. Table 9shows the results. The maximum absorption wavelength (λmax) was measuredunder the following conditions.

Spectrophotometer: Self-recording spectrophotometer (trade name: U-3300;manufactured by Hitachi, Ltd.)

Measurement cell: 1 cm quartz cell

Sampling interval: 0.1 nm

Scanning rate: 30 nm/min

Number of measurements: Measurement was performed five times to take theaverage value of the five measurements.

(4) Creation of Recorded Product

Each of the inks A1 to G4 thus prepared was mounted on an ink jetrecording apparatus (trade name: Pixus 950i; manufactured by CANON Inc.)to print a 13-level gradation pattern on an ink jet glossy medium (tradename: PR101; manufactured by CANON Inc.) by changing a printing duty to5, 12, 21, 29, 35, 43, 51, 58, 66, 74, 85, 90, and 100%. Thus, arecorded product was created.

(5) Evaluation of Bronze Resistance

The printing duty at which the bronze phenomenon occurred in the13-level gradation pattern of the recorded product thus created wasvisually observed to define the printing duty as the printing duty atwhich the bronze phenomenon occurred. In general, the bronze phenomenonis apt to occur with increasing the printing duty. In other words, thebronze phenomenon is more likely to occur where the ink has a lowerprinting duty at which the bronze phenomenon occurs, while the bronzephenomenon is less likely to occur where the ink has a higher printingduty at which the bronze phenomenon occurs. The criteria for the bronzeresistance are as follows. Table 9 shows the results of the evaluation.

-   A: The printing duty at which the bronze phenomenon occurs is 55% or    more.-   B: The printing duty at which the bronze phenomenon occurs is 40% or    more and less than 55%.-   C: The printing duty at which the bronze phenomenon occurs is 35% or    more and less than 40%.-   D: The printing duty at which the bronze phenomenon occurs is less    than 35%.

(6) Evaluation of Environmental Gas Resistance

The recorded product thus created was placed in an ozone test apparatus(trade name: OMS-H; manufactured by SUGA TEST INSTRUMENTS) to performozone exposure in an environment having a temperature of 40° C., ahumidity of 55%, and an ozone gas concentration of 2 ppm for 20 hours. Aremaining density ratio was calculated on the basis of the followingexpression (3) from the reflection densities at a 50% duty portion ofthe recorded product before and after the exposure test. The reflectiondensities were measured by means of a Macbeth RD-918 (manufactured byMacbeth). The criteria for the environmental gas resistance are asfollows. Table 9 shows the results of the evaluation.Remaining density ratio=(d ₀₃ /d _(ini))×100 (%)  Eq. (3)(in the expression (3), d₀₃ represents the reflection density after theozone exposure and d_(ini) represents the reflection density before theozone exposure.)

-   A: A remaining density ratio of 83% or more.-   B: A remaining density ratio of less than 83%.

TABLE 9 Maximum d₇₅ absorption value wavelength Bronze Environmental Ink[nm] λ max[nm] resistance gas resistance Example A1 7.51 612.0 A A A27.50 611.9 A A B1 10.59 608.1 B A B2 10.60 608.0 B A C1 6.71 612.9 A AC2 6.72 612.8 A A Comparative A3 7.52 611.8 C A Example A4 7.52 611.7 CA B3 10.60 608.0 C A B4 10.61 607.9 C A C3 6.73 612.7 C A C4 6.71 612.6C A D1 10.61 607.9 C A D2 10.62 607.8 C A D3 10.63 607.7 D A D4 10.63607.7 D A E1 6.69 613.1 A B E2 6.68 613.2 A B E3 6.69 613.1 A B E4 6.68613.2 A B F1 14.38 603.0 D A F2 14.39 602.9 D A F3 14.39 602.9 D A F414.40 602.8 D A G1 6.00 614.0 A B G2 6.01 613.9 A B G3 6.02 613.8 A B G46.03 613.6 A B

In accordance with the above results, the following was confirmed. Inthe case where the coloring material of the present invention which is acompound represented by the general formula (I) or a salt thereof isused, environmental gas resistance may not be sufficient when the d₇₅value of ink is smaller than 6.70 nm, and bronze resistance may not besufficient when the d₇₅ value is larger than 10.60 nm. Based on theabove results, it was also confirmed that excellent bronze resistancecould be obtained in the case where the content (mass %) of2-pyrrolidone among the water-soluble organic solvents is 50.0% or morewith respect to the content (mass %) of the coloring material.

The present application claims the priority from each of Japanese PatentApplication No. 2004-196451 filed on Jul. 2, 2004 and Japanese PatentApplication No. 2005-192190 filed on Jun. 30, 2005, which are herebyincorporated by reference herein.

1. An ink jet ink comprising at least water, a water-soluble organicsolvent and a coloring material, wherein the coloring material is acompound represented by the following general formula (1) or a saltthereof; a content (mass %) of the coloring material is 0.5 mass % ormore and less than 3.0 mass % with respect to a total mass of the inkjet ink; and a content (mass %) of 2-pyrrolidone in the water-solubleorganic solvent is 50.0% or more with respect to the content (mass %) ofthe coloring material; and in a dispersion distance distribution,measured by a small-angle X-ray scattering method, of molecularaggregates in the ink jet ink whose coloring material concentration isadjusted to 0.5 mass %, a dispersion distance d₇₅ value corresponding to75% of the distribution is 6.70 nm or more and 10.60 nm or less:

wherein M represents an alkali metal or ammonium; R₁ and R₂ eachindependently represent a hydrogen atom, a sulfonic group, or a carboxylgroup provided that R₁ and R₂ are not simultaneously a hydrogen atom; Yrepresents a chlorine atom, a hydroxyl group, an amino group, or amonoalkylamino or dialkylamino group; 1 represents 0 to 2, m represents1 to 3, and n represents 1 to 3 provided that 1+m+n=3 to 4); andpositions at which substituents are present are the 4- or 4′-positions.2. An ink jet ink according to claim 1, wherein the coloring material isa compound represented by the following general formula (II) or a saltthereof:

wherein M represents an alkali metal or ammonium; 1 represents 0 to 2, mrepresents 1 to 3, and n represents 1 to 3 provided that 1+m+n=3 to 4;and positions at which substituents are present are the 4- or4′-positions.
 3. An ink jet ink according to claim 1, wherein thecoloring material contains at least the compound in which 1≧1.
 4. An inkjet ink according to claim 1, wherein the d₇₅ value is 9.10 nm or less.5. An ink jet recording method, comprising ejecting an ink by an ink jetmethod to perform recording on a recording medium, wherein the inkcomprises the ink jet ink according to claim
 1. 6. An ink cartridge,comprising an ink storage portion for storing ink, wherein the inkcomprises the ink jet ink according to claim
 1. 7. A recording unit,comprising an ink storage portion for storing ink and a recording headfor ejecting the ink, wherein the ink comprises the ink jet inkaccording to claim
 1. 8. An ink jet recording apparatus, comprising anink storage portion for storing ink and a recording head for ejectingthe ink, wherein the ink comprises the ink jet ink according to claim 1.9. An ink jet ink comprising at least water, a water-soluble organicsolvent and a coloring material, wherein the coloring material is acompound represented by the following general formula (I) or a saltthereof; a content (mass %) of the coloring material is 0.5 mass % ormore and less than 3.0 mass % with respect to a total mass of the inkjet ink; and a content (mass %) of 2-pyrrolidone in the water-solubleorganic solvent is 50.0% or more with respect to the content (mass %) ofthe coloring material; and a maximum absorption wavelength (λmax)obtained by measuring an absorbance of an ink prepared by diluting 2,000times the ink jet ink is 608.0 nm or more and 613.0 nm or less:

wherein M represents an alkali metal or ammonium; R₁ and R₂ eachindependently represent a hydrogen atom, a sulfonic group, or a carboxylgroup provided that R₁ and R₂ are not simultaneously a hydrogen atom; Yrepresents a chlorine atom, a hydroxyl group, an amino group, or amonoalkylamino or dialkylamino group; 1 represents 0 to 2, m represents1 to 3, and n represents 1 to 3 provided that 1+m+n=3 t 4; and positionsat which substituents are present are the 4- or 4′-positions.
 10. An inkjet ink according to claim 9, wherein the coloring material is acompound represented by the following general formula (II) or a saltthereof

wherein M represents an alkali metal or ammonium; 1 represents 0 to 2, mrepresents 1 to 3, and n represents 1 to 3 provided that 1+m+n=3 to 4;and positions at which substituents are present are the 4- or4′-positions.
 11. An ink jet ink according to claim 9, wherein thecoloring material contains at least the compound in which 1≧1.
 12. Anink jet ink according to claim 9, wherein the maximum absorptionwavelength (λmax) is 610.0 nm or more and 613.0 nm or less.
 13. An inkjet recording method, comprising ejecting an ink by an ink jet method toperform recording on a recording medium, wherein the ink comprises theink jet ink according to claim
 9. 14. An ink cartridge, comprising anink storage portion for storing ink, wherein the ink comprises the inkjet ink according to claim
 9. 15. A recording unit, comprising an inkstorage portion for storing ink and a recording head for ejecting theink, wherein the ink comprises the ink jet ink according to claim
 9. 16.An ink jet recording apparatus, comprising an ink storage portion forstoring ink and a recording head for ejecting the ink, wherein the inkcomprises the ink jet ink according to claim 9.